Commitment To Quality
Product innovation has been the key driver to our global success and understanding the science eventually helps us develop better compounds to combat disease, which has immensely shaped our competitive edge on the global platform.
G J Pharmaceuticals LLP
has pioneered in transforming unique business ideas into complete logical solutions encompassing, designing and formulation development of innovative and effective lifesaving medicines that make a significant difference in the real life situations of the people around the globe. State-of-the-art testing and analytical equipment at multiple locations, which facilitate investigations into a wide range of chemistries and substrates through a variety of methods.
Regulatory Affairs Department is the main strength of Pharmaceutical Business :
Our Regulatory team consists of highly qualified personnel engaged in providing data required as per the Regulatory Guidelines of the different countries. Our Regulatory Team can provide a complete support to register the Products.
We Can Also Provide You
- CTD Dossiers
- ACTD Dossiers
- Dossiers as per specific Guideline of all countries
- Bio-Equivalence Studies with GLP certified clinical centers (BE Study)
- Pharmacokinetic Studies,
- Drug master Files (DMF)
- Site Master File
- Electronic Submission of Dossiers with all supporting documents
Certificate of Pharmaceutical Product (as per WHO), USFDA , EU Certificate , Free Sale Certificates, Certificate of Origin, Halal Certificates, Kosher Certificates, TSE-BSE Certificates.